Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy.

The IAAM/IAAM haplotype showed a trend of association to later DCM onset (>50% DCM-free patients at last follow-up vs. 20.0 years at median onset, n = 16 and 150 respectively, log-rank p = 0.15) ( Fig 2C ).

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